Publication date: 15th December 2025
Self-assembled monolayers (SAMs) have previously been shown to perform well as hole-selective layers in solution-processed organic solar cells (OSCs) [1-5]. In this work, we investigated the feasibility of several common spin-coated carbazole SAMs – 2PACz, MeO-2PACz, and Br-2PACz, spanning a range of HOMO levels and work functions from about -4.5 to -6 eV – for integration in vacuum processed fullerene-based OSCs with DTDCPB or DCV4T as donor molecules, with HOMO energies of approximately –5.4 and –5.8 eV respectively. We found that certain SAMs increased the power conversion efficiency of the DTDCPB and DCV4T OSCs by up to 20% and 13% respectively relative to that of our control devices with a standard MoOx hole contact: this relative enhancement in performance was linked to improvements in open circuit voltage (VOC) which occurred if the HOMO of the SAM was below that of the donor. We used capacitance voltage measurements to directly determine the built-in voltage (Vbi) of each OSC and demonstrated that the trend in Vbi closely follows the VOC and the energetic alignment of the different SAMs relative to each donor. These results can be used to help guide future SAM-donor combinations in OSCs. As vacuum thermal evaporation is a readily-scalable fabrication method [6], we seek to make fully evaporated SAM-based OSCs. In preparation for this, we attempted to evaporate the aforementioned SAMs. We have so far found that Br-2PACz degraded during attempted evaporation, but we were able to successfully evaporate 2PACz, in agreement with literature [7]. In this presentation, we aim to compare the fully evaporated device stacks to their solution processed counterparts. We will also complete complementary characterisation to confirm the same energetic changes occur, and we plan to attempt stability testing on these devices.
K. T. is funded by the Clarendon Scholarship, awarded in partnership with the Waverley Scholarship and she thanks the Clarendon Fund; The Queen’s College, Oxford; and the Waverley Fund for their support. We acknowledge the EPSRC National Thin Film Facility for Advanced Functional Materials (NTCF), hosted by the Department of Physics at the University of Oxford, and Dr Jin Yao and Dr Matthew Naylor, the facility engineers for their support. The NTCF was funded by ESPRC (EP/M022900/1), the Wolfson Foundation and the University of Oxford. H. N. acknowledges the EPSRC for funding his Vacation Internship. P. K. thanks EPSRC for funding for a Postdoctoral Fellowship (no. EP/V035770/1) and Linacre College for the award of a Junior Research Fellowship. O.J.S. acknowledges funding from the Research Council of Finland through Project No. 357196. M. N. acknowledges funding from The Swedish Cultural Foundation in Finland.
